scholarly journals Diffusion tensor imaging of white matter and correlates to eye movement control and psychometric testing in children with prenatal alcohol exposure

2016 ◽  
Vol 38 (1) ◽  
pp. 444-456 ◽  
Author(s):  
Angelina Paolozza ◽  
Sarah Treit ◽  
Christian Beaulieu ◽  
James N. Reynolds
2015 ◽  
Vol 27 (4) ◽  
pp. 197-205 ◽  
Author(s):  
Kirsten Ann Donald ◽  
Annerine Roos ◽  
Jean-Paul Fouche ◽  
Nastassja Koen ◽  
Fleur M. Howells ◽  
...  

BackgroundNeuroimaging studies have indicated that prenatal alcohol exposure is associated with alterations in the structure of specific brain regions in children. However, the temporal and regional specificity of such changes and their behavioural consequences are less known. Here we explore the integrity of regional white matter microstructure in infants with in utero exposure to alcohol, shortly after birth.MethodsTwenty-eight alcohol-exposed and 28 healthy unexposed infants were imaged using diffusion tensor imaging sequences to evaluate white matter integrity using validated tract-based spatial statistics analysis methods. Second, diffusion values were extracted for group comparisons by regions of interest. Differences in fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD) and radial diffusivity were compared between groups and associations with measures from the Dubowitz neonatal neurobehavioural assessment were examined.ResultsLower AD values (p<0.05) were observed in alcohol-exposed infants in the right superior longitudinal fasciculus compared with non-exposed infants. Altered FA and MD values in alcohol-exposed neonates in the right inferior cerebellar were associated with abnormal neonatal neurobehaviour.ConclusionThese exploratory data suggest that prenatal alcohol exposure is associated with reduced white matter microstructural integrity even early in the neonatal period. The association with clinical measures reinforces the likely clinical significance of this finding. The location of the findings is remarkably consistent with previously reported studies of white matter structural deficits in older children with a diagnosis of foetal alcohol spectrum disorders.


2015 ◽  
Vol 36 (6) ◽  
pp. 2318-2329 ◽  
Author(s):  
Prapti Gautam ◽  
Catherine Lebel ◽  
Katherine L. Narr ◽  
Sarah N. Mattson ◽  
Philip A. May ◽  
...  

2021 ◽  
Author(s):  
Preeti Kar ◽  
Jess E. Reynolds ◽  
Melody N. Grohs ◽  
W. Ben Gibbard ◽  
Carly McMorris ◽  
...  

Prenatal alcohol exposure (PAE) can lead to cognitive, behavioural, and social-emotional challenges. Previous neuroimaging research has identified alterations to brain structure in newborns, older children, adolescents, and adults with PAE; however, little is known about brain structure in young children. Extensive brain development takes place during early childhood; therefore, understanding the neurological profiles of young children with PAE is critical for early identification and effective intervention. We studied 54 children (5.21 +/- 1.11 years; 27 males) with confirmed PAE compared to 54 age- and sex-matched children without PAE. Children underwent diffusion tensor imaging between 2 and 7 years of age. Mean fractional anisotropy (FA) and mean diffusivity (MD) were obtained for 10 major white matter tracts, along with tract volume, axial and radial diffusivity (AD, RD). A univariate analysis of covariance was conducted to test for group differences (PAE vs. control) controlling for age, sex and tract volume. Our results reveal white matter microstructural differences between young children with PAE and unexposed controls. The PAE group had higher FA and/or lower MD (as well as lower AD and RD) in the genu and the body of the corpus callosum, as well as the bilateral uncinate fasciculus and pyramidal tracts. Our findings align with studies of newborns with PAE finding lower AD, but contrast those in older populations with PAE, which consistently report lower FA and higher MD. These findings may reflect premature development of white matter that may then plateau too early, leading to the lower FA/higher MD observed at older ages.


2015 ◽  
Vol 36 (7) ◽  
pp. 2470-2482 ◽  
Author(s):  
Jia Fan ◽  
Ernesta M. Meintjes ◽  
Christopher D. Molteno ◽  
Bruce S. Spottiswoode ◽  
Neil C. Dodge ◽  
...  

2021 ◽  
pp. 153537022098039
Author(s):  
Erin Mathews ◽  
Kevyn Dewees ◽  
Deborah Diaz ◽  
Carlita Favero

Fetal Alcohol Spectrum Disorders (FASDs) describe a range of deficits, affecting physical, mental, cognitive, and behavioral function, arising from prenatal alcohol exposure. FASD causes widespread white matter abnormalities, with significant alterations of tracts in the cerebral cortex, cerebellum, and hippocampus. These brain regions present with white-matter volume reductions, particularly at the midline. Neural pathways herein are guided primarily by three guidance cue families: Semaphorin/Neuropilin, Netrin/DCC, and Slit/Robo. These guidance cue/receptor pairs attract and repulse axons and ensure that they reach the proper target to make functional connections. In several cases, these signals cooperate with each other and/or additional molecular partners. Effects of alcohol on guidance cue mechanisms and their associated effectors include inhibition of growth cone response to repellant cues as well as changes in gene expression. Relevant to the corpus callosum, specifically, developmental alcohol exposure alters GABAergic and glutamatergic cell populations and glial cells that serve as guidepost cells for callosal axons. In many cases, deficits seen in FASD mirror aberrancies in guidance cue/receptor signaling. We present evidence for the need for further study on how prenatal alcohol exposure affects the formation of neural connections which may underlie disrupted functional connectivity in FASD.


NeuroImage ◽  
2014 ◽  
Vol 102 ◽  
pp. 748-755 ◽  
Author(s):  
Wei Cao ◽  
Wei Li ◽  
Hui Han ◽  
Shonagh K. O'Leary-Moore ◽  
Kathleen K. Sulik ◽  
...  

Author(s):  
Preeti Kar ◽  
Jess E. Reynolds ◽  
Melody N. Grohs ◽  
W. Ben Gibbard ◽  
Carly McMorris ◽  
...  

2021 ◽  
pp. 108826
Author(s):  
Annerine Roos ◽  
Catherine J. Wedderburn ◽  
Jean-Paul Fouche ◽  
Sivenesi Subramoney ◽  
Shantanu H. Joshi ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document